Select Publications
Book Chapters
2019, '9 Synthesis and applications of backbone-fluorinated amino acids', in Fluorine in Life Sciences: Pharmaceuticals, Medicinal Diagnostics, and Agrochemicals, Elsevier, pp. 325 - 347, http://dx.doi.org/10.1016/b978-0-12-812733-9.00009-x
,2018, 'Synthesis and applications of backbone-fluorinated amino acids', in Fluorine in Life Sciences: Pharmaceuticals, Medicinal Diagnostics, and Agrochemicals Progress in Fluorine Science Series, pp. 325 - 347, http://dx.doi.org/10.1016/B978-0-12-812733-9.00009-X
,2017, 'Total Synthesis of Ustiloxin D', in Harmata M (ed.), Strategies and Tactics in Organic Synthesis, Elsevier, pp. 169 - 191, http://dx.doi.org/10.1016/B978-0-08-100756-3.00006-6
,2017, 'β-Fluoroamines (Update 2017)', in Science of Synthesis, pp. 413 - 444, http://dx.doi.org/10.1055/sos-SD-134-00206
,2016, 'Chapter 6 Total Synthesis of Ustiloxin D', in , Elsevier, pp. 169 - 191, http://dx.doi.org/10.1016/b978-0-08-100756-3.00006-6
,Journal articles
2024, 'Precious Cargo: The Role of Polymeric Nanoparticles in the Delivery of Covalent Drugs', Molecules, 29, http://dx.doi.org/10.3390/molecules29204949
,2024, 'The influence of backbone fluorination on the helicity of α/γ-hybrid peptides', Organic and Biomolecular Chemistry, 22, pp. 1608 - 1612, http://dx.doi.org/10.1039/d3ob02016a
,2023, 'Tinker, Tailor, Soldier, Spy: The Diverse Roles That Fluorine Can Play within Amino Acid Side Chains', Molecules, 28, http://dx.doi.org/10.3390/molecules28176192
,2021, 'Fluorinated quorum sensing inhibitors: enhancement of potency through conformational control', Organic and Biomolecular Chemistry, 19, pp. 9629 - 9636, http://dx.doi.org/10.1039/d1ob01649k
,2021, 'The effect of vicinal difluorination on the conformation and potency of histone deacetylase inhibitors', Molecules, 26, pp. 3974, http://dx.doi.org/10.3390/molecules26133974
,2021, 'Analytical-scale synthesis of aryl-SF
2021, 'Discovery of neuroprotective agents that inhibit human prolyl hydroxylase PHD2', Bioorganic and Medicinal Chemistry, 38, http://dx.doi.org/10.1016/j.bmc.2021.116115
,2021, 'Controlling γ-Peptide Helicity with Stereoselective Fluorination', European Journal of Organic Chemistry, 2021, pp. 1184 - 1190, http://dx.doi.org/10.1002/ejoc.202001619
,2021, 'Synthesis of phenazine-2,8-dicarboxylates', Arkivoc, 2022, http://dx.doi.org/10.24820/ARK.5550190.P011.661
,2020, 'Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids', Organic and Biomolecular Chemistry, 18, pp. 8192 - 8198, http://dx.doi.org/10.1039/d0ob01811b
,2020, 'Strategies for Fine-Tuning the Conformations of Cyclic Peptides', Chemical Reviews, 120, pp. 9743 - 9789, http://dx.doi.org/10.1021/acs.chemrev.0c00013
,2020, 'Predicting Octanol-Water Partition Coefficients of Fluorinated Drug-Like Molecules: A Combined Experimental and Theoretical Study', Australian Journal of Chemistry, 73, pp. 677 - 685, http://dx.doi.org/10.1071/CH19648
,2020, 'Revisiting inflammatory bowel disease: Pathology, treatments, challenges and emerging therapeutics including drug leads from natural products', Journal of Clinical Medicine, 9, http://dx.doi.org/10.3390/jcm9051273
,2020, 'Vicinal difluorination as a C=C surrogate: An analog of piperine with enhanced solubility, photostability, and acetylcholinesterase inhibitory activity', Beilstein Journal of Organic Chemistry, 16, pp. 2663 - 2670, http://dx.doi.org/10.3762/BJOC.16.216
,2019, 'Correction: The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research (Natural Product Reports (2018) DOI: 10.1039/c7np00064b)', Natural Product Reports, 36, pp. 248 - 249, http://dx.doi.org/10.1039/c8np90041h
,2019, 'In pursuit of fluorinated sigma receptor ligand candidates related to [ 18 F]-FPS', Australian Journal of Chemistry, 72, pp. 213 - 225, http://dx.doi.org/10.1071/CH18510
,2019, 'The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research', Natural Product Reports, 36, pp. 35 - 107, http://dx.doi.org/10.1039/c7np00064b
,2019, 'Tuning the properties of a cyclic RGD-containing tetrapeptide through backbone fluorination', Organic and Biomolecular Chemistry, 17, pp. 664 - 674, http://dx.doi.org/10.1039/c8ob02679c
,2018, 'Synthesis and biochemical characterisation of fluorinated analogues of pepstatin A and grassystatin A', Tetrahedron, 74, pp. 1278 - 1287, http://dx.doi.org/10.1016/j.tet.2017.12.033
,2017, 'Recent Developments in the Deoxyfluorination of Alcohols and Phenols: New Reagents, Mechanistic Insights, and Applications', Synthesis (Germany), 49, pp. 4917 - 4930, http://dx.doi.org/10.1055/s-0036-1590881
,2017, 'Homologated amino acids with three vicinal fluorines positioned along the backbone: Development of a stereoselective synthesis', Beilstein Journal of Organic Chemistry, 13, pp. 2316 - 2325, http://dx.doi.org/10.3762/bjoc.13.228
,2017, 'Synthesis and Determination of the pK
2017, 'Cyclic peptide unguisin A is an anion receptor with high affinity for phosphate and pyrophosphate', Organic and Biomolecular Chemistry, 15, pp. 2962 - 2967, http://dx.doi.org/10.1039/C7OB00316A
,2016, 'Scalable, stereoselective syntheses of α,β-difluoro-γ-amino acids', Tetrahedron, 72, pp. 3305 - 3317, http://dx.doi.org/10.1016/j.tet.2016.04.070
,2016, 'Concise Synthesis of Dictyoquinazol A via a Dimerisation-Cyclocondensation Sequence', Synlett, 27, pp. 1237 - 1240, http://dx.doi.org/10.1055/s-0035-1561569
,2016, 'Synthesis and neuroprotective activity of dictyoquinazol A and analogues', Bioorganic and Medicinal Chemistry, 24, pp. 1480 - 1487, http://dx.doi.org/10.1016/j.bmc.2016.02.016
,2016, 'Diastereoselective Synthesis and Conformational Analysis of (2R)- and (2S)-Fluorostatines: An Approach Based on Organocatalytic Fluorination of a Chiral Aldehyde', Organic Letters, 18, pp. 662 - 665, http://dx.doi.org/10.1021/acs.orglett.5b03592
,2016, 'ChemInform Abstract: Concise Synthesis of Dictyoquinazol A via a Dimerisation—Cyclocondensation Sequence.', ChemInform, 47, http://dx.doi.org/10.1002/chin.201640213
,2015, 'Investigation of cis- and trans-4-Fluoroprolines as Enantioselective Catalysts in a Variety of Organic Transformations', Australian Journal of Chemistry, 68, pp. 44 - 49, http://dx.doi.org/10.1071/CH14129
,2015, 'Probing the Mode of Neurotransmitter Binding to GABA Receptors Using Selectively Fluorinated GABA Analogues', Australian Journal of Chemistry, 68, pp. 23 - 30, http://dx.doi.org/10.1071/CH14456
,2015, 'ChemInform Abstract: A D‐Ribose‐Derived α‐Amino Nitrile as a Versatile Intermediate for the Collective Synthesis of Piperidine‐Type Iminosugar C‐Glycosides.', ChemInform, 46, http://dx.doi.org/10.1002/chin.201517263
,2014, 'A d-ribose-derived α-amino nitrile as a versatile intermediate for the collective synthesis of piperidine-type iminosugar C-glycosides', Tetrahedron Letters, 55, pp. 7222 - 7225, http://dx.doi.org/10.1016/j.tetlet.2014.11.024
,2014, 'ChemInform Abstract: Stereoselectively Fluorinated N‐Heterocycles: A Brief Survey', ChemInform, 45, http://dx.doi.org/10.1002/chin.201440259
,2014, 'Incrementally increasing the length of a peptide backbone: Effect on macrocyclisation efficiency', Organic and Biomolecular Chemistry, 12, pp. 4598 - 4601, http://dx.doi.org/10.1039/c4ob00492b
,2014, 'Total synthesis and antiplasmodial activity of pohlianin C and analogues', Bioorganic and Medicinal Chemistry Letters, 24, pp. 2645 - 2647, http://dx.doi.org/10.1016/j.bmcl.2014.04.071
,2014, 'Stereoselective fluorination alters the geometry of a cyclic peptide: Exploration of backbone-fluorinated analogues of unguisin a', Angewandte Chemie - International Edition, 53, pp. 6176 - 6179, http://dx.doi.org/10.1002/anie.201403071
,2014, 'Stereoselective Fluorination Alters the Geometry of a Cyclic Peptide: Exploration of Backbone‐Fluorinated Analogues of Unguisin A', Angewandte Chemie, 126, pp. 6290 - 6293, http://dx.doi.org/10.1002/ange.201403071
,2014, 'Radio-opaque micelles for X-ray imaging', Australian Journal of Chemistry, 67, pp. 78 - 84, http://dx.doi.org/10.1071/CH13391
,2014, 'Conformational regulation of substituted azepanes through mono-, di-, and trifluorination', European Journal of Organic Chemistry, 2014, pp. 2584 - 2593, http://dx.doi.org/10.1002/ejoc.201301811
,2014, 'ChemInform Abstract: Sequential Deoxyfluorination Approach for the Synthesis of Protected α,β,γ‐Trifluoro‐δ‐amino Acids.', ChemInform, 45, http://dx.doi.org/10.1002/chin.201413220
,2013, 'Stereoselectively fluorinated N-heterocycles: A brief survey', Beilstein Journal of Organic Chemistry, 9, pp. 2696 - 2708, http://dx.doi.org/10.3762/bjoc.9.306
,2013, 'Sequential deoxyfluorination approach for the synthesis of protected α,β,γ-trifluoro-δ-amino acids', Organic Letters, 15, pp. 5562 - 5565, http://dx.doi.org/10.1021/ol402756e
,2013, 'Conformational regulation of substituted azepanes through selective monofluorination.', Org. Biomol. Chem., 11, pp. 3781 - 3785, http://dx.doi.org/10.1039/c3ob40391b
,2012, 'ChemInform Abstract: α,β‐Difluoro‐γ‐amino Acids — Synthesis and Applications', ChemInform, 43, http://dx.doi.org/10.1002/chin.201243251
,2012, 'alpha,beta-Difluoro-gamma- amino acids Synthesis and applications', CHIMICA OGGI-CHEMISTRY TODAY, 30, pp. 20 - 22, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000305146800004&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
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